Silicon Reagents for Organic Synthesis pp 58-78 | Cite as
Peterson Reaction
Chapter
Abstract
The Silyl-Wittig or Peterson reaction involves addition of a stoichiometric quantity of an α-silyl carbanion to the carbonyl group of a ketone or aldehyde. This yields a β-silyl alkoxide which decomposes by alkoxide attack on silicon to yield an alkene and a silanoate. The ease of this decomposition is dependent on the cation. Potassium and sodium alkoxides decompose far more readily than the more covalent magnesium alkoxides [1].
Keywords
Grignard Reagent Trimethylsilyl Group Magnesium Bromide Vinyl Silane Vinyl Sulfide
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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